| A
G-Quadruplex DNA Cleaving Compound and Novel DNA-Cleaving Antitumor
Agents
Introduction
There have been few dramatic therapeutic
breakthroughs in cancer research. More anticancer drugs are
in use today than ever before, but nearly all of these drugs
are severely limited in their use, due to the dual problems
of drug resistance and lack of selectivity. The guanine-rich
ends of chromosomes, the telomeres, are prime targets for
anticancer agents. The DNA in these regions of the genome
are believed to be capable of forming G-quadruplex structures,
yet no known compound exists that might recognize and selectively
cleave these unique DNA structures. It is postulated that
G-quadruplex structures are more prevalent in cancer cells
than normal cells, providing a means of selectivity in treatment.
Invention Description
This invention describes a new compound
that selectively cleaves G-quadruplex DNA. This compound may
have applications in the treatment of cancer and other proliferative
diseases. We show that compound I is selective for G-quadruplex
DNA and leaves duplex DNA relatively unharmed. A significant
advantage of this compound from the therapeutic point of view
is that water-soluble sodium salts of this compound can be
readily formulated.
A method for treating cancer involving
the use of novel compounds is described and claimed as new
compositions of matter. The utility of these compounds for
the treatment of cancer stems from the way that they interact
with DNA. These compounds are non-hydrolyzable, cationic compounds
that bind to DNA. They also undergo a series of chemical reactions
in the presence of DNA to generate reactive intermediates
that cleave the DNA. These compounds may selectively localize
to cancer cells due to their lipophilic, cationic nature.
Thus, these compounds are exciting new candidates for cancer
therapeutic treatment.
Benefits
- These drugs are readily taken up by
cancer cells.
- Importantly, these compounds cleave
DNA structures prevalent in cancer cells.
- High selectivity allows exposure of
cells and animals to compounds with little toxicity concerns.
Features
- New anticancer drug compositions
- Can be refined through high-throughput
screening
- Cancer cells are affected by specific
interactions with DNA structures prevalent in telomeric
domains
Market Potential/Applications
Cancer is the second leading cause of
death in the United States. Each year, over half a million
Americans die from cancer. The global cancer market is predicted
to be around $20 billion in 2004, and is expected to increase
to over $45 billion by 2011. Over the next decade, advances
in the pharmacotherapy of cancer will come not only from improvements
in the traditional classes of therapies, but also from introduction
of innovative therapies such as this one, that display improved
efficacy and toxicity through a targeted approach.
Development Stage
Proof of concept completed
RDF
IP Status
Three U.S. Patents issued
11 Foreign Patent Applications filed
UT Researcher
Sean Kerwin, Ph.D., College of Pharmacy,
The University of Texas at Austin
Wendi David, Ph.D., Chemistry and Biochemistry, Texas State
University
For further information please contact:
University of Texas,
Austin, USA
Website : www.otc.utexas.edu

|